Variant report

Variant	nsv875576
Chromosome Location	chr2:188343497-188482933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3479)
CpG islands
(count:549)
Chromatin interactive
region (count:132)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3479 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188365601-188366189	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:188459686-188459815	K562	blood:	n/a	n/a
3	ARID3A	chr2:188417779-188418437	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:188411457-188411585	K562	blood:	n/a	n/a
5	ARID3A	chr2:188416243-188416679	K562	blood:	n/a	n/a
6	ARID3A	chr2:188364564-188365077	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:188362488-188362990	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:188445189-188446578	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:188417188-188419388	K562	blood:	n/a	n/a
10	ARID3A	chr2:188376745-188376936	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:188439872-188439983	K562	blood:	n/a	n/a
12	ARID3A	chr2:188405710-188407124	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:188411998-188413154	K562	blood:	n/a	n/a
14	ARID3A	chr2:188378261-188378460	HepG2	liver:	n/a	n/a
15	ARID3A	chr2:188394446-188395361	HepG2	liver:	n/a	n/a
16	ARID3A	chr2:188441711-188441904	K562	blood:	n/a	n/a
17	ARID3A	chr2:188414692-188415523	HepG2	liver:	n/a	n/a
18	ARID3A	chr2:188414115-188414413	HepG2	liver:	n/a	n/a
19	ARID3A	chr2:188410134-188410334	HepG2	liver:	n/a	n/a
20	ARID3A	chr2:188412186-188412528	HepG2	liver:	n/a	n/a
21	ARID3A	chr2:188391976-188392625	HepG2	liver:	n/a	n/a
22	ARID3A	chr2:188364484-188365250	K562	blood:	n/a	chr2:188365216-188365232
23	ARID3A	chr2:188374294-188375172	HepG2	liver:	n/a	n/a
24	ARID3A	chr2:188445260-188446786	K562	blood:	n/a	n/a
25	ARID3A	chr2:188362596-188363368	K562	blood:	n/a	n/a
26	ARID3A	chr2:188382504-188382798	HepG2	liver:	n/a	n/a
27	ATF1	chr2:188461274-188461426	K562	blood:	n/a	n/a
28	ATF1	chr2:188381359-188381631	K562	blood:	n/a	n/a
29	ATF1	chr2:188451755-188452052	K562	blood:	n/a	n/a
30	ATF1	chr2:188412101-188412457	K562	blood:	n/a	n/a
31	ATF1	chr2:188374620-188375115	K562	blood:	n/a	n/a
32	ATF1	chr2:188417828-188418218	K562	blood:	n/a	n/a
33	ATF2	chr2:188364673-188364992	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr2:188404393-188405200	HCT-116	colon:	n/a	chr2:188404612-188404623 chr2:188404614-188404622
35	ATF3	chr2:188445228-188445831	K562	blood:	n/a	n/a
36	ATF3	chr2:188412043-188412645	HCT-116	colon:	n/a	n/a
37	ATF3	chr2:188412092-188412532	A549	lung:	n/a	n/a
38	ATF3	chr2:188445322-188445922	A549	lung:	n/a	n/a
39	ATF3	chr2:188406218-188406907	A549	lung:	n/a	n/a
40	ATF3	chr2:188412011-188412662	HCT-116	colon:	n/a	n/a
41	ATF3	chr2:188417772-188418260	K562	blood:	n/a	n/a
42	ATF3	chr2:188365430-188366172	A549	lung:	n/a	n/a
43	ATF3	chr2:188412053-188412480	K562	blood:	n/a	n/a
44	ATF3	chr2:188365526-188366189	A549	lung:	n/a	n/a
45	ATF3	chr2:188412150-188412417	K562	blood:	n/a	n/a
46	ATF3	chr2:188406176-188407188	A549	lung:	n/a	n/a
47	ATF3	chr2:188394594-188395445	A549	lung:	n/a	n/a
48	BACH1	chr2:188395959-188396172	K562	blood:	n/a	n/a
49	BACH1	chr2:188411517-188411587	K562	blood:	n/a	n/a
50	BACH1	chr2:188407802-188407916	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188419568-188419618	MCF10A-Er-Src	breast:	n/a
2	chr2:188419830-188419880	HUVEC	blood vessel:	n/a
3	chr2:188419933-188419983	GM12892	blood:	n/a
4	chr2:188391145-188391195	K562	blood:	n/a
5	chr2:188481707-188481757	GM12891	blood:	n/a
6	chr2:188378844-188378894	SAEC	small airway:	n/a
7	chr2:188391145-188391195	SKMC	muscle:	n/a
8	chr2:188391145-188391195	GM06990	blood:	n/a
9	chr2:188481707-188481757	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:188378844-188378894	LNCaP	prostate:	n/a
11	chr2:188378844-188378894	HNPCEpiC	eye:	n/a
12	chr2:188419933-188419983	AoSMC	blood vessel:	n/a
13	chr2:188419087-188419137	AoSMC	blood vessel:	n/a
14	chr2:188419568-188419618	PANC-1	pancreas:	n/a
15	chr2:188419087-188419137	HMEC	breast:	n/a
16	chr2:188419933-188419983	NT2-D1	testis:	n/a
17	chr2:188419830-188419880	Hepatocyte	liver:	n/a
18	chr2:188419568-188419618	SK-N-MC	brain:	n/a
19	chr2:188420266-188420316	AG04449	skin:	fetal
20	chr2:188378844-188378894	SK-N-SH	brain:	n/a
21	chr2:188378844-188378894	CMK	blood:	n/a
22	chr2:188419830-188419880	SKMC	muscle:	n/a
23	chr2:188419830-188419880	GM12892	blood:	n/a
24	chr2:188481707-188481757	PANC-1	pancreas:	n/a
25	chr2:188419568-188419618	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:188419830-188419880	MCF-7	breast:	n/a
27	chr2:188481707-188481757	AG04450	lung:	fetal
28	chr2:188419933-188419983	HMEC	breast:	n/a
29	chr2:188391145-188391195	LNCaP	prostate:	n/a
30	chr2:188391145-188391195	HepG2	liver:	n/a
31	chr2:188419830-188419880	GM06990	blood:	n/a
32	chr2:188406934-188406984	HCT-116	colon:	n/a
33	chr2:188419087-188419137	SK-N-SH	brain:	n/a
34	chr2:188419933-188419983	AG09309	skin:	n/a
35	chr2:188378844-188378894	HEEpiC	esophagus:	n/a
36	chr2:188420266-188420316	GM06990	blood:	n/a
37	chr2:188419933-188419983	K562	blood:	n/a
38	chr2:188419568-188419618	NHDF-neo	bronchial:	n/a
39	chr2:188419087-188419137	GM12892	blood:	n/a
40	chr2:188378844-188378894	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:188481707-188481757	SAEC	small airway:	n/a
42	chr2:188419933-188419983	AG10803	skin:	n/a
43	chr2:188481707-188481757	HNPCEpiC	eye:	n/a
44	chr2:188378844-188378894	AoSMC	blood vessel:	n/a
45	chr2:188419933-188419983	SKMC	muscle:	n/a
46	chr2:188419933-188419983	RPTEC	kidney:	n/a
47	chr2:188419568-188419618	Jurkat	blood:	n/a
48	chr2:188378844-188378894	MCF-7	breast:	n/a
49	chr2:188391145-188391195	HCPEpiC	choroid plexus:	n/a
50	chr2:188391145-188391195	GM12878	blood:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:188398970..188401688-chr2:188404214..188406089,3	K562	blood:
2	chr2:188395123..188398204-chr2:188399307..188403080,4	K562	blood:
3	chr2:188382536..188387002-chr2:188394148..188396925,4	K562	blood:
4	chr2:188349779..188351933-chr2:188354447..188356243,2	K562	blood:
5	chr2:188349831..188352709-chr2:188404428..188405999,2	K562	blood:
6	chr2:187752239..187754172-chr2:188437559..188440188,2	K562	blood:
7	chr2:188387495..188389336-chr2:188392022..188394869,2	MCF-7	breast:
8	chr2:187749024..187750695-chr2:188416544..188418279,2	K562	blood:
9	chr2:188392650..188395033-chr2:188412614..188414418,2	K562	blood:
10	chr2:188367231..188371096-chr2:188401019..188405423,6	K562	blood:
11	chr2:188365827..188368256-chr2:188403673..188406049,2	MCF-7	breast:
12	chr2:188365429..188366272-chr2:188444751..188446554,9	K562	blood:
13	chr2:188364934..188367555-chr2:188418302..188420499,2	K562	blood:
14	chr2:188363780..188367877-chr2:188441342..188445875,5	MCF-7	breast:
15	chr2:188362272..188363211-chr2:188445966..188446643,3	MCF-7	breast:
16	chr2:188364663..188366800-chr2:188416557..188418283,2	K562	blood:
17	chr2:188361661..188363462-chr2:188407026..188409234,2	K562	blood:
18	chr2:188329317..188331418-chr2:188341720..188346261,4	K562	blood:
19	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
20	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
21	chr2:188353320..188355812-chr2:188357936..188360335,2	K562	blood:
22	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
23	chr2:188449920..188452608-chr2:188452638..188454975,2	K562	blood:
24	chr2:188363934..188366778-chr2:188370276..188373007,2	K562	blood:
25	chr2:188362272..188363211-chr2:188445966..188446643,3	MCF-7	breast:
26	chr2:188366746..188369254-chr2:188412378..188414717,2	K562	blood:
27	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
28	chr2:188362271..188363016-chr2:188446864..188447543,2	MCF-7	breast:
29	chr2:188412314..188413944-chr2:188414421..188417624,3	MCF-7	breast:
30	chr2:188343524..188345048-chr2:188346989..188348629,2	K562	blood:
31	chr2:188440243..188443082-chr2:188444632..188448024,3	K562	blood:
32	chr2:188338540..188341601-chr2:188345636..188349487,3	K562	blood:
33	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
34	chr2:188375111..188377616-chr2:188395627..188398222,2	K562	blood:
35	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
36	chr2:188351020..188353616-chr2:188354924..188357575,2	K562	blood:
37	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
38	chr2:188443788..188447797-chr2:188450278..188454059,4	K562	blood:
39	chr2:188393262..188398014-chr2:188414587..188419751,6	K562	blood:
40	chr1:146713788..146714307-chr2:188445941..188446637,2	MCF-7	breast:
41	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
42	chr2:188363922..188366266-chr2:188444694..188447033,35	MCF-7	breast:
43	chr2:188362083..188363643-chr2:188369549..188371149,2	K562	blood:
44	chr2:188343524..188345048-chr2:188346989..188348629,2	K562	blood:
45	chr2:188367651..188372772-chr2:188414874..188419301,6	K562	blood:
46	chr2:188389696..188391580-chr2:188402374..188405162,2	K562	blood:
47	chr2:188363929..188365341-chr2:188444758..188446502,16	K562	blood:
48	chr2:188408868..188410387-chr2:188412786..188414991,2	MCF-7	breast:
49	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
50	chr2:263068..264963-chr2:188441341..188443685,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-1	chr2:188418876-188418918	ENSG00000224063.1
2	lnc-FAM171B-1	chr2:188419003-188419120	ENSG00000224063.1
3	lnc-FAM171B-1	chr2:188419304-188419390	ENSG00000224063.1

No data

Variant related genes	Relation type
TFPI	TF binding region
ENSG00000224063	TF binding region
TFPI	CpG island
ENSG00000224063	CpG island
ENSG00000131778	chromatin interactions
ENSG00000035115	chromatin interactions
ENSG00000224063	chromatin interactions
ENSG00000003436	chromatin interactions
ENSG00000143727	chromatin interactions

Extended variants
information (count: 4376 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:4376 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7586970	chr2:188343497-188343498	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs144664871	chr2:188343515-188343516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs267599118	chr2:188343519-188343520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554858342	chr2:188343521-188343522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs8176532	chr2:188343534-188343535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576298696	chr2:188343548-188343549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199893386	chr2:188343569-188343570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568300304	chr2:188343575-188343576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559141356	chr2:188343620-188343621	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577356943	chr2:188343637-188343638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541560048	chr2:188343658-188343659	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559544463	chr2:188343693-188343694	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367615991	chr2:188343704-188343705	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs8176531	chr2:188343707-188343708	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561191190	chr2:188343721-188343722	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531669431	chr2:188343722-188343723	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs8176530	chr2:188343734-188343735	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116350534	chr2:188343762-188343763	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7576066	chr2:188343781-188343782	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs8176529	chr2:188343816-188343817	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547479084	chr2:188343840-188343841	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370278854	chr2:188343903-188343904	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183947531	chr2:188343919-188343920	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547812172	chr2:188343932-188343933	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569295361	chr2:188343945-188343946	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537389193	chr2:188343988-188343989	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547878259	chr2:188344025-188344026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566144368	chr2:188344118-188344119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188726765	chr2:188344149-188344150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115056211	chr2:188344162-188344163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534867472	chr2:188344168-188344169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369810253	chr2:188344171-188344172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548522122	chr2:188344185-188344186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574959454	chr2:188344197-188344198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375460811	chr2:188344202-188344203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542325772	chr2:188344210-188344211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114006673	chr2:188344223-188344224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575704127	chr2:188344257-188344258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58477172	chr2:188344308-188344309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180686081	chr2:188344314-188344315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35837997	chr2:188344316-188344317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34056716	chr2:188344343-188344344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543701328	chr2:188344352-188344353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564992588	chr2:188344407-188344408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144692632	chr2:188344468-188344469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375058961	chr2:188344500-188344501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111438521	chr2:188344515-188344516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112471286	chr2:188344519-188344520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559475648	chr2:188344533-188344534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559701038	chr2:188344574-188344575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188326800-188353600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr2:188326800-188357600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:188326800-188357800	Weak transcription	Lung	lung
4	chr2:188327000-188357800	Weak transcription	Left Ventricle	heart
5	chr2:188327200-188357600	Weak transcription	Fetal Intestine Large	intestine
6	chr2:188328200-188357600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr2:188328200-188360000	Weak transcription	Psoas Muscle	Psoas
8	chr2:188328400-188365400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr2:188328600-188357200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr2:188329000-188358000	Weak transcription	K562	blood
11	chr2:188329200-188347800	Strong transcription	Liver	Liver
12	chr2:188330600-188344400	Weak transcription	Fetal Lung	lung
13	chr2:188332800-188357600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:188334200-188374600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr2:188334600-188348200	Weak transcription	A549	lung
16	chr2:188336800-188344200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:188336800-188345800	Strong transcription	HUVEC	blood vessel
18	chr2:188337200-188354000	Strong transcription	HepG2	liver
19	chr2:188339400-188349600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:188339800-188357600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:188340800-188343800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr2:188341000-188344400	Strong transcription	Placenta	Placenta
23	chr2:188341200-188344000	Strong transcription	NHDF-Ad	bronchial
24	chr2:188341200-188347200	Strong transcription	NH-A	brain
25	chr2:188341200-188349400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:188341200-188357200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr2:188341400-188343600	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr2:188341800-188343800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:188341800-188345400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:188342200-188346000	Weak transcription	Adipose Nuclei	Adipose
31	chr2:188342200-188350600	Strong transcription	Osteobl	bone
32	chr2:188342400-188344000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr2:188342600-188356600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:188342800-188343600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:188342800-188347200	Weak transcription	NHLF	lung
36	chr2:188342800-188347400	Weak transcription	HSMMtube	muscle
37	chr2:188342800-188348200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:188342800-188357200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr2:188342800-188362400	Strong transcription	HSMM	muscle
40	chr2:188343400-188343800	Strong transcription	Fetal Muscle Leg	muscle
41	chr2:188343400-188347600	Weak transcription	Hela-S3	cervix
42	chr2:188343400-188348400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr2:188343600-188344000	Genic enhancers	Muscle Satellite Cultured Cells	--
44	chr2:188343600-188346000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:188343800-188346200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:188343800-188347600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:188343800-188357600	Weak transcription	Fetal Muscle Leg	muscle
48	chr2:188344000-188348400	Weak transcription	NHDF-Ad	bronchial
49	chr2:188344000-188348800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:188344000-188349600	Strong transcription	Muscle Satellite Cultured Cells	--

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